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KRT18P10 keratin 18 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 360019, updated on 17-Sep-2024

Summary

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Official Symbol
KRT18P10provided by HGNC
Official Full Name
keratin 18 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:23962
See related
Ensembl:ENSG00000214207 AllianceGenome:HGNC:23962
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See KRT18P10 in Genome Data Viewer
Location:
Yp11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (5573089..5574488)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (5253097..5254496)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (5441130..5442529)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene protocadherin 11 Y-linked Neighboring gene voltage dependent anion channel 1 pseudogene 6 Neighboring gene NANOG hESC enhancer GRCh37_chrY:5192864-5193440 Neighboring gene eukaryotic translation initiation factor 4A1 pseudogene 2 Neighboring gene sorting nexin 3 pseudogene 1 Y-linked Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrY:5577568-5578528 Neighboring gene ribosomal protein L26 pseudogene 37

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Skaletsky H, et al. Nature, 2003 Jun 19. PMID 12815422
  2. Toward a complete human genome sequence. Sanger Center, et al. Genome Res, 1998 Nov. PMID 9847074

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_002937.5 

    Range
    101..1500
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    5573089..5574488
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    5253097..5254496
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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